α-Thalassemia and Hereditary Spherocytosis in the Same Patient: The Interaction of two Diseases
Author:
Publisher
Informa UK Limited
Subject
Oncology,Hematology,Pediatrics, Perinatology, and Child Health
Link
http://www.tandfonline.com/doi/pdf/10.3109/08880019809028796
Reference9 articles.
1. Multiple Inherited Erythrocyte Abnormalities in an American Negro Family: Hereditary Spherocytosis, Sickling and Thalassemia
2. The Combination of Hereditary Spherocytosis and Heterozygous Beta-Thalassaemia
3. Occurrence of hereditary spherocytosis and β thalassaemia in the same family: globin chain synthesis and visco diffractometric studies
4. Coexistence of hereditary spherocytosis (HS) due to band 3 deficiency and β-thalassaemia trait: partial correction of HS phenotype
5. Interaction of Hereditary Spherocytosis and Alpha Thalassaemia: A Family Study
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1. The coincidence of beta‐thalassemia and hereditary spherocytosis: A case report and literature review;Clinical Case Reports;2024-06
2. Peripheral Blood Smear Findings in 2 Patients With Coexisting Thalassemia and Hereditary Spherocytosis;Journal of Pediatric Hematology/Oncology;2022-09-13
3. α‑thalassaemia combined with hereditary spherocytosis in the same patient;Experimental and Therapeutic Medicine;2017-11-28
4. A New α1-Globin Mutation, Hb Brugg [α20(B1)His→Gln];Hemoglobin;2011-07-28
5. Iron and iron proteins found in the genetic disease, hereditary spherocytosis;Inorganica Chimica Acta;2002-11
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